Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians (2008)
- Authors:
- Autor USP: ISAAC, LOURDES - ICB
- Unidade: ICB
- Assunto: IMUNOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Investigative Ophthalmology and Visual Science
- Volume/Número/Paginação/Ano: v. 49, 2008
- Conference titles: Annual Meeting of the Association for Research in Vision and Ophthalmology - ARVO
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ABNT
TEIXEIRA, A. et al. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. St. Louis: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 17 nov. 2024. , 2008 -
APA
Teixeira, A., Silva, A. S., Lin, F. L. H., Isaac, L., & Belfort, R. (2008). Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. St. Louis: Instituto de Ciências Biomédicas, Universidade de São Paulo. -
NLM
Teixeira A, Silva AS, Lin FLH, Isaac L, Belfort R. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. 2008 ; 49[citado 2024 nov. 17 ] -
Vancouver
Teixeira A, Silva AS, Lin FLH, Isaac L, Belfort R. Association of the Y402H polymorphism in complement factor h gene and age-related macular degeneration in brazilians. Investigative Ophthalmology and Visual Science. 2008 ; 49[citado 2024 nov. 17 ] - Seria a alfa 2 macroglobulina uma proteina de fase aguda no camundongo?
- Células do sistema imune
- Structural requirements for thioester bond formation in human omplement component c3
- Requisitos estruturais para a formacao da ligacao tio-ester no componente c3 do sistema complemento
- Concentrations of complement proteins in brazilian healthy children and adults
- Simple method to distinguish between primary and secondary C3 deficiencies
- New human c3 deficient case
- Complement C3 deficiency and evidence of nonsense-codon mediated decay
- Homozygous factor h deficiency
- An intriguing case of primary complement C3 deficiency
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